Guanfacine
NDC Package 68094-019-62

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Guanfacine is a . Marketed by Precision Dose, Inc., this product is identified by NDC 68094-019 and is authorized under FDA application ANDA075109.

Identification & Billing

NDC Package Code
68094-019-62
Package Description
3 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK (68094-019-59)
Product Code
68094-019
11-Digit Billing Format
68094001962
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
3 EA

Clinical Specifications

Proprietary Name
Guanfacine
Dosage Form
-

Regulatory & Marketing

Labeler Name
Precision Dose, Inc.
FDA Application #
ANDA075109
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
08-05-2019
End Marketing Date
06-30-2022
Listing Expiration
06-30-2022
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 68094-019-62 identifies a specific commercial package of 3 blister pack in 1 carton / 10 tablet in 1 blister pack (68094-019-59) of Guanfacine, labeled by Precision Dose, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Precision Dose, Inc. on August 05, 2019. The current certification is valid through June 30, 2022.

How is this Precision Dose, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68094001962. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 3 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
68094-019-62
11-Digit CMS (5-4-2)
68094-0019-62

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.